Gotowe bibliografie tematyczne / Thiourea derivatives

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  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji

Gotowa bibliografia na temat „Thiourea derivatives”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Thiourea derivatives"

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Ngaini, Zainab, Wan Sharifatun Handayani Wan Zulkiplee, and Ainaa Nadiah Abd Halim. "One-Pot Multicomponent Synthesis of Thiourea Derivatives in Cyclotriphosphazenes Moieties." Journal of Chemistry 2017 (2017): 1–7. http://dx.doi.org/10.1155/2017/1509129.

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In this study, hexasubstituted thiourea was carried out via reaction of isothiocyanato cyclophosphazene intermediates with a series of aromatics amines and amino acids in a one-pot reaction system. The reaction was not as straightforward as typical thiourea synthesis. Six unexpected thiourea derivatives3a–fwere formed in the presence of cyclotriphosphazene moieties in good yields (53–82%). The structures of3a–fwere characterized by elemental analysis and FTIR,1H,13C, and31P NMR spectroscopies. The occurrence of reverse thioureas formation in a one-pot reaction system is discussed. The possible
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Al-Riyahee, Ali A. A. "First Row Transition Metal Complexes Derived from N, Nʹ-Substituted Thiourea: Synthesis, Geometrical Structures and Cyclic Voltammetry Probe: A Review". BASRA JOURNAL OF SCIENCE 39, № 1 (2021): 96–118. http://dx.doi.org/10.29072/basjs.202117.

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Thioureas or thiourea derivatives as organosulfur compounds are one of the most widely used ligands in different applications as we are going to discuss it extensively such as in coordination chemistry by involving them to rich sources of N, O and S atoms coordinating through S atom, S and O atoms in benzoyl derivatives or S, O and N atoms in pyridyl hetrocylic benzoyl derivatives. These hard and soft donor sites facilitate the bonding between thiourea free ligand and metal ion through one or more to make ligands behave as mono, bi or multidentate ligands to form huge and stable series of the
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Elshaier, Yaseen A. M. M., Ashraf A. Aly, Mohamed Abdel-Aziz, et al. "Synthesis and Identification of New N,N-Disubstituted Thiourea, and Thiazolidinone Scaffolds Based on Quinolone Moiety as Urease Inhibitor." Molecules 27, no. 20 (2022): 7126. http://dx.doi.org/10.3390/molecules27207126.

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Synthesis of thiazolidinone based on quinolone moiety was established starting from 4-hydroxyquinol-2-ones. The strategy started with the reaction of ethyl bromoacetate with 4-hydroxyquinoline to give the corresponding ethyl oxoquinolinyl acetates, which reacted with hydrazine hydrate to afford the hydrazide derivatives. Subsequently, hydrazides reacted with isothiocyanate derivatives to give the corresponding N,N-disubstituted thioureas. Finally, on subjecting the N,N-disubstituted thioureas with dialkyl acetylenedicarboxylates, cyclization occurred, and thiazolidinone derivatives were obtain
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Binzet, Gun, Bülent Zeybek, Esma Kılıç, Nevzat Külcü, and Hakan Arslan. "Determination of the Ionization Constants of Some Benzoyl Thiourea Derivatives in Dioxane-Water Mixture." Journal of Chemistry 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/201238.

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The stoichiometric ionization constants ofN,N-dialkyl-N′-(4-substituted benzoyl) thiourea (Substitutes: H, Cl, and Br; alkyl groups: ethyl,n-propyl,n-butyl, and phenyl) derivatives have been determined potentiometrically in dioxane-water (v:v, 50:50) mixture at ionic strength of 0.1 M and25.0±0.1°C. The ionization constants were calculated with the BEST computer program and the formation curves using the data obtained from the potentiometric titrations. The effects of substituents and alkyl groups on the ionization constants of the benzoyl thiourea derivatives have been investigated. A compari
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Makhsumov, Abduhamid, Yusubjon Holboyev, Nailya Valeeva, Boburbek Ismailov, and Ibragim Askarov. "Synthesis of 1-nicotinoylo-3-(meta-nitrophenyl)- thiourea derivatives with anti-inflammatory activity." E3S Web of Conferences 434 (2023): 02032. http://dx.doi.org/10.1051/e3sconf/202343402032.

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Thiourea derivatives are used in many industries: medicine, agriculture, engineering, rubber industry, organic synthesis. On their basis, various preparations for the needs of the national economy were obtained. The latest studies of thiourea derivatives, carried out at the present time, are prompted not only by theoretical, but also by practical needs. From this point of view, thiourea derivatives are of undoubted interest in substances with different biological activities. They are widely used in agriculture and have been used as herbicides, fungicides, insecticides, bactericides, dyes, grow
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Kovalskaya, A. V., A. N. Lobov, V. V. Zarubaev, and I. P. Tsypysheva. "Derivatives of (–)-Cytisine with Thiourea Fragment. Synthesis and Antiviral Activity." Žurnal obŝej himii 94, no. 6 (2024): 712–21. http://dx.doi.org/10.31857/s0044460x24060054.

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New derivatives of the quinolizidine alkaloid, (–)-cytisine, with a substituted 2-pyridone ring and a thiourea moiety in the bispidin fragment of the molecule were synthesized. The ability of the synthesized cytisine-containing thioureas to inhibit the reproduction of human parainfluenza virus type 3 was assessed. It was found that the derivatives obtained by the reaction of benzoyl or phenyl isothiocyanate with (–)-cytisine, as well as its 9-bromo or 9,11-derivative, effectively suppress the reproduction of human parainfluenza virus type 3 (their selectivity indices are 56, 58 and 95, respect
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Viana, Gil Mendes, Edézio Ferreira da Cunha-Junior, Paloma Wetler Meireles Carreiros Assumpção, et al. "Synthesis and Structure–Activity Relationship of Thiourea Derivatives Against Leishmania amazonensis." Pharmaceuticals 17, no. 12 (2024): 1573. http://dx.doi.org/10.3390/ph17121573.

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Background: Leishmaniasis, caused by Leishmania protozoa and transmitted by vectors, presents varied clinical manifestations based on parasite species and host immunity. The lack of effective vaccines or treatments has prompted research into new therapies, including thiourea derivatives, which have demonstrated antiprotozoal activities. Methods: We synthesized two series of N,N′-disubstituted thiourea derivatives through the reaction of isothiocyanates with amines. These compounds were evaluated in vitro against promastigote and amastigote forms of L. amazonensis, alongside cytotoxicity assess
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Binzet, Gün, Gülten Kavak, Nevzat Külcü, Süheyla Özbey, Ulrich Flörke, and Hakan Arslan. "Synthesis and Characterization of Novel Thiourea Derivatives and Their Nickel and Copper Complexes." Journal of Chemistry 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/536562.

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New benzoyl thiourea derivatives and their nickel and copper complexes were synthesized. The structure of the synthesized compounds were confirmed by elemental analysis, FT-IR, and1H NMR techniques. Four of the synthesized compounds are analyzed by X-ray single crystal diffraction technique. WhereasN,N-dimethyl-N′-(4-fluorobenzoyl)thiourea,N,N-diethyl-N′-(4-fluorobenzoyl)thiourea, andN,N-di-n-butyl-N′-(4-fluorobenzoyl) thiourea crystallize in the monoclinic system,bis(N,N-di-n-propyl-N′-(4-fluorobenzoyl)thioureato) nickel(II) complex crystallizes in the triclinic system. These ligand molecules
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Venkatachalam, TK, Elise A. Sudbeck, Chen Mao, and Fatih M. Uckun. "Piperidinylethyl, Phenoxyethyl and Fluoroethyl Bromopyridyl Thiourea Compounds with Potent Anti-HIV Activity." Antiviral Chemistry and Chemotherapy 11, no. 5 (2000): 329–36. http://dx.doi.org/10.1177/095632020001100503.

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Derivatives of piperidinylethyl, phenoxyethyl and fluoroethyl bromopyridyl thioureas were designed and synthesized as non-nucleoside reverse transcriptase inhibitors (NNRTIs) of HIV-1 reverse transcriptase (RT). The anti-HIV activity of these compounds was examined by determining their ability to inhibit the replication of the HIV-1 strain HTLVIIIB in human peripheral blood mononuclear cells. The unsubstituted parent pyridyl thiourea compound N-[2-(1-piperidine)ethyl]-N′-[2-(pyridyl)] thiourea (1) exhibited no anti-HIV activity, even at 100 μM. However, the thiourea derivatives that contain a
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Erol Günal, Şule, and Engin Kaplan. "SYNTHESIS, EVALUATION OF ANTIFUNGAL ACTIVITY AND DRUG-LIKENESS OF BENZOYL THIOUREA DERIVATIVES." İstanbul Ticaret Üniversitesi Fen Bilimleri Dergisi 24, no. 47 (2025): 217–28. https://doi.org/10.55071/ticaretfbd.1588118.

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Herein, we report the synthesis of a series of 2-bromobenzoyl-substituted thiourea derivatives. The structures of the synthesized thioureas were characterized by spectroscopic methods. These derivatives, together with 2-fluorobenzoyl thioureas synthesized previously, have been evaluated for their potential antifungal activity. Compounds 2d and 2f showed antifungal activity against Candida albicans. Compound 2f also demonstrated activity against C. parapsilosis. Drug-likeness properties of the compounds were also estimated, and it was found that all compounds showed good drug-likeness propertie
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Rozprawy doktorskie na temat "Thiourea derivatives"

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Apps, James Frederick Shuan-Liang. "Synthesis and application of thiourea-S,S-dioxide derivatives." Thesis, University of Warwick, 2008. http://wrap.warwick.ac.uk/53126/.

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The structure and synthesis of N,N'-disubstituted thiourea-S,S-dioxides were investigated experimentally and computationally. Hydrogen peroxide oxidation of acyclic and cyclic N,N'-dialkylthioureas furnished S,S-dioxides in agreement with computational predictions. Some s,S,S-trioxides were also isolated. An X-ray crystallographic study of N,N'-diisopropylthiourea dioxide, fIrst synthesised in this work, verilled computational models. The prediction of a stable N,N'-diarylthiourea dioxide derivative was supported by successful isolation of the dioxide. The application of N,N'-diisopropylthiour
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Rampalakos, Konstantinos. "Asymmetric synthesis with vapol derivatives and novel chiral thiourea organocatalysts." Diss., Connect to online resource - MSU authorized users, 2008.

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Hof, Kira [Verfasser]. "Non-Covalent organocatalysis utilizing thiourea derivatives : understanding and creating organocatalyzed reactions / Kira Hof." Gießen : Universitätsbibliothek, 2014. http://d-nb.info/1068589736/34.

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Saglam, Guluzar. "Synthesis Of Novel Chiral Thiourea Derivatives And Their Applications, Synthesis Of Some Hdac Inhibitors, Addition Of Acyl Phosphonates To Ethylcyanoformate." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/3/12609265/index.pdf.

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The thiourea derivatives have become a main focus of research in asymmetric synthesis as an organocatalyst in recent years. In the first part, the thiourea catalysts are synthesized starting from easily available L-tartaric acid and application of the catalysts to some addition reactions showed no significant asymmetric induction. A number of HDAC inhibitors have been developed as anti-cancer agent at the present time.In the second part, some aryl butenoic acid derivatives are synthesized as HDAC inhibitors starting from substituted benzaldehyde and pyruvic acid. The HDAC activity studies sho
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Chandanshive, Jay Zumbar <1983&gt. "Regiocontrolled Synthesis of Pyrazole Derivatives Through 1,3-Dipolar Cycloaddition Reaction And Synthesis of Helicene-Thiourea based and Polymer Supported Soos's Catalyst for Asymmetric Synthesis." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5826/1/Chandanshive_JAY_ZUMBAR_Thesis.pdf.

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In first part we have developed a simple regiocontrolled protocol of 1,3-DC to get ring fused pyrazole derivatives. These pyrazole derivatives were synthesized using 1,3-DC between nitrile imine and various dipolarophiles such as alkynes, cyclic α,β-ketones, lactones, thiocatones and lactums. The reactions were found to be highly regiospecific. In second part we have discussed about helicene, its properties, synthesis and applications as asymmetric catalyst.Due to inherent chirality, herein we have made an attempt to synthesize the helicene-thiourea based catalyst for asymmetric catalysi
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Chandanshive, Jay Zumbar <1983&gt. "Regiocontrolled Synthesis of Pyrazole Derivatives Through 1,3-Dipolar Cycloaddition Reaction And Synthesis of Helicene-Thiourea based and Polymer Supported Soos's Catalyst for Asymmetric Synthesis." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2013. http://amsdottorato.unibo.it/5826/.

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In first part we have developed a simple regiocontrolled protocol of 1,3-DC to get ring fused pyrazole derivatives. These pyrazole derivatives were synthesized using 1,3-DC between nitrile imine and various dipolarophiles such as alkynes, cyclic α,β-ketones, lactones, thiocatones and lactums. The reactions were found to be highly regiospecific. In second part we have discussed about helicene, its properties, synthesis and applications as asymmetric catalyst.Due to inherent chirality, herein we have made an attempt to synthesize the helicene-thiourea based catalyst for asymmetric catalysi
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Guan, Qiao-Zhi, and 官巧之. "Synthesis of Chiral Isoxazole Derivatives Employing Bifunctional Thiourea Organocatalyst and 1,5-difluoro-2,4-dinitrobenzene." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/04658731297954677104.

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碩士<br>國立臺灣師範大學<br>化學系<br>99<br>This thesis deals with the synthesis of biologically active chiral bicyclic isoxazole and isoxazoline derivatives. The synthetic methodology involves two steps. In the first step, β-nitrostyrene derivatives were treated with allyl or propargyl malonates in the presence of chiral bifunctional thiourea catalyst to obtain the corresponding optically active Michael adducts. The resultant chiral Michael adducts were treated with DBU and 1,5-difluoro-2,4-dinitrobenzene (DFDNB) to generate nitrile oxides in situ. The nitrile oxide intermediates underwent intramolecular
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Wan-yu, Lin, and 林宛諭. "Synthesis Chiral Isoxazole Derivatives via 1,3-dipolar Cycloaddition from Michael Adducts by Using Difucntional Thiourea an Organocatalyst." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/90147113050256226100.

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碩士<br>國立臺灣師範大學<br>化學系<br>100<br>Isoxazole and isoxazoline derivatives are common and can be found in the nature compounds. The isoxazole derivatives structure are stable and facilitate for variety synthesis as intermediates. In medical system, enantiomeric isoxazole and isoxazoline are used in therapeutic process. Therefore, it becomes major tasks for synthesis enantiomeric isoxazole and isoxazoline. We have recently prepared nitrostyrene and dimethyl allyl malonate (and dimethyl propargyl malonate) with additive chiral bifunctional thiourea for 1,4-Michael addition. With H-bonding, the thiour
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Morifi, E. L. "Cobalt and cadmium chalcogenide nanomaterials from complexes based on thiourea, urea and their alkyl derivatives : synthesis and characterization." Thesis, 2015. http://hdl.handle.net/10352/302.

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M. Tech. (Department of Chemistry, Faculty of Applied and Computer Science), Vaal University of Technology<br>Cadmium and cobalt complexes of urea and thiourea were synthesized using ethanol as a solvent. All complexes were refluxed at 70 - 80 °C, left to cool at room temperature, washed with methanol and acetone to remove impurities and dried at an open environment. The characterization of complexes was done using FTIR spectroscopy, elemental analysis and TGA. The complexes were found to coordination with the ligands through sulphur and oxygen atoms to the metal, instead of nitrogen. These we
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Lethobane, Manthako Hycinth. "The synthesis and characterization of ZnS nanoparticles from zinc-based thiourea derivative complexes for potential use in photocatalysis." Thesis, 2017. https://hdl.handle.net/10539/25002.

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A dissertation submitted to the Faculty of Science, University of the Witwatersrand in partial fulfilment of the requirement for the degree Master of Science (M.Sc.) in Chemistry. Johannesburg, 31 October 2017.<br>Nanotechnology has been instrumental in finding strategies of combating some of the world’s grand challenges. Water scarcity and the growing industrialization have made it an imperative to find ways of cleaning water. Photocatalysis is a promising method for water purification personified by the use of solar energy as well as nanomaterials with tailored properties. Colloidal synthes
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Książki na temat "Thiourea derivatives"

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Arpe, Hans-Jürgen. Surgical Materials to Thiourea and Thiourea Derivatives, Volume A26, Ullmann's Encyclopedia of Industrial Chemistry. 5th ed. Wiley-VCH, 1995.

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Części książek na temat "Thiourea derivatives"

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Barcelo, Jose-Manuel, Maria-Rosario Rosillo, and José Luis García-Abujeta. "Contact Dermatitis Due to Thiourea Derivatives." In Encyclopedia of Medical Immunology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-9194-1_575.

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Song, Baoan, Linhong Jin, Song Yang, and Pinaki S. Bhadury. "Synthesis and Antiviral Activity of Chiral Thiourea Derivatives." In Environment-Friendly Antiviral Agents for Plants. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-03692-7_4.

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Filipowska, Anna, Wojciech Filipowski, and Ewaryst Tkacz. "Study of Structure-Cytotoxicity Relationships of Thiourea Derivatives Containing the 2-Aminothiazole Moiety." In Innovations in Biomedical Engineering. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-47154-9_32.

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Filipowska, Anna, Wojciech Filipowski, Ewaryst Tkacz, and Monika Wujec. "Statistical Analysis of the Impact of Molecular Descriptors on Antimicrobial Activity of Thiourea Derivatives Incorporating 3-amino-1,2,4-triazole Scaffold." In Innovations in Biomedical Engineering. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-70063-2_19.

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Zade, Chetan M., Umesh D. Pete, Megharaj S. Kadam, and Ratnamala S. Bendre. "Development of Novel Insect Growth Regulators: Effect of 1-(Substitutedbenzoyl)-3-[(2′-Isopropyl-5′-Methylphenoxy) Acetamino] Thiourea and Urea Derivatives on Total Haemocyte Count of Dysdercus koenigii." In Chemistry for Sustainable Development. Springer Netherlands, 2011. http://dx.doi.org/10.1007/978-90-481-8650-1_5.

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Kausar, Samia, Ataf Ali Altaf, Muhammad Hamayun, Amin Badshah, and Abdul Razzaq. "Supramolecular Chemistry and DNA Interaction Studies of Ferrocenyl Ureas and Thioureas." In Photophysics, Photochemical and Substitution Reactions- Recent Advances [Working Title]. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.84412.

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In this chapter, we have discussed the characteristics and bioapplicabilities of different ferrocene derivatives, for example, amides, amines, sulfonamide, and polymers, focusing mainly on urea and thiourea derivatives due to their autonomous and widespread spectroscopic action and bioactivities. Supramolecular chemistry of ferrocenyl ureas and thioureas is described owing to exploring their mode of interactions within and among the molecules and the role of these supramolecular structures in enhancing the DNA intercalation. DNA interaction studies of these ferrocenyl-based ureas and thioureas
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Hof, K., K. M. Lippert, and P. R. Schreiner. "Nonstereoselective Transformations with Achiral Thiourea Derivatives." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00208.

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Hof, K., K. M. Lippert, and P. R. Schreiner. "Stereoselective Transformations with Chiral Thiourea Derivatives." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00209.

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Ito, S., and N. Morita. "Condensation Reactions with S-Methylated Thiourea Derivatives." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-00399.

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Hof, K., K. M. Lippert, and P. R. Schreiner. "Thiourea Derivatives as Organocatalysts in Organic Synthesis." In Brønsted Base and Acid Catalysts, and Additional Topics. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-205-00207.

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Streszczenia konferencji na temat "Thiourea derivatives"

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K, Venkata Muralidhar, Vinay Jain, and Beena Rai. "Thiourea Derivatives as Steel Corrosion Inhibitors: Density Functional Theory and Experimental Studies." In CORROSION 2019. NACE International, 2019. https://doi.org/10.5006/c2019-13317.

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Abstract Thiourea and its derivatives have been studied for several decades, for their corrosion inhibition characteristics with steels. However, their interaction mechanisms with steel are not well understood. Such an understanding may be vital for design of novel thiourea derivatives as corrosion inhibitors for steels. We have carried out state of the art density functional theory (DFT) computations and experiments (weightloss, polarization and electrochemical impedance) to understand the effect of thioureas on corrosion of steel. The interactions of thiourea and dibutyl thiourea separately
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Nedeljković, Nikola V., Vladimir D. Dobričić, Marina Ž. Mijajlović, et al. "„IN SILICO“ PREDICTION OF PHARMACOKINETIC PROPERTIES AND DRUGLIKENESS OF NOVEL THIOUREA DERIVATIVES OF NAPROXEN." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.371n.

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Masking the carboxyl group of naproxen with other functional groups may be a promising strategy to decrease its gastrointestinal toxicity. Thiourea moiety has been described as an important pharmacophore in a variety of pharmacologically active compounds, including anti-inflammatory, antiviral, anticancer, hypoglycemic and antimicrobial agents. Our research group has previously designed twenty novel thiourea derivatives of naproxen, containing amino acids (glycine, L-alanine, β-alanine, L-valine and L-phenylalanine – compounds 1,2,3,4 and 5, respectively), their methyl (6–10) and ethyl esters
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Fakhar, Imran, Bohari M. Yamin, and Siti Aishah Hasbullah. "Synthesis and characterization of bis-thiourea having amino acid derivatives." In THE 2016 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2016 Postgraduate Colloquium. Author(s), 2016. http://dx.doi.org/10.1063/1.4966750.

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Nikolić, Miloš, Marina Mijajlović, and Nikola Nedeljković. "Anti-Inflammatory Screening of Thiourea Derivatives Based on Molecular Docking Studies." In Sinteza 2022. Singidunum University, 2022. http://dx.doi.org/10.15308/sinteza-2022-365-372.

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Nedeljković, Nikola V., Vladimir D. Dobričić, Marina Ž. Vesović, et al. "In silico estimation of COX-2 and 5-LOX inhibitory potential of some novel thiourea derivatives of naproxen." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.475n.

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Design of dual COX-2/5-LOX inhibitors can be considered an adequate approach in the development of new anti-inflammatory drugs with less pronounced side effects. The aim of the present research was to examine the binding potential of the seven newly designed thiourea derivatives of naproxen towards COX-2 and 5-LOX. The binding analysis of ligand conformations was performed by OEDocking 3.2.0.2 software. The binding potential assessment revealed that thiourea derivatives of naproxen exhibited a comparable binding affinity as naproxen towards COX-2. The highest number of key binding interactions
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Korkmaz, Neslihan, Stephen Astley, and Demet Astley. "SYNTHESIS AND CHARACTERISATION OF NOVEL CHIRAL THIOUREA DERIVATIVES AS POTENTIAL BIOLOGICAL ACTIVE AGENTS." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00671.

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Silva*, Claudia Brito da, and Fabiano Severo Rodembusch. "Synthesis and spectroscopic characterization of urea/thiourea derivatives for potential optical sensors application." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201310114206.

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Nikolić, Miloš, Vladimir Dobričić, Nikola Nedeljković, Marina Mijajlović, and Zorica Vujić. "Molecular docking analysis of novel thiourea derivatives of naproxen with potential antitumor activity." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07436.

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Umapriya, Kollu, Avula Vijaya Kumar Reddy, Vallela Swetha, Grigory V. Zyryanov, and Chamarthi Naga Raju. "Antioxidant activity of urea/thiourea derivatives of 5-methyl-3-(urediomethyl)-hexanoic acid." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069017.

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Nedeljković, Nikola, Vladimir Dobričić, Marina Mijajlović, Zorica Vujić, and Miloš Nikolić. "Molecular Docking Analysis of Novel Thiourea Derivatives of Naproxen with Potential Anti-Inflammatory Activity." In ECMC 2022. MDPI, 2022. http://dx.doi.org/10.3390/ecmc2022-13279.

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